Cargando…
Dabrafenib: a new opportunity for the treatment of BRAF V600-positive melanoma
Prior to 2011, the 1-year survival rates for patients suffering from advanced or metastatic melanoma was as low as 33%, with a median overall survival of about 9 months. Several chemotherapeutic regimens have been applied, either as monochemotherapy or as polychemotherapy, overall not resulting in a...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4866744/ https://www.ncbi.nlm.nih.gov/pubmed/27226731 http://dx.doi.org/10.2147/OTT.S75104 |
_version_ | 1782431960277188608 |
---|---|
author | Banzi, Maria De Blasio, Simona Lallas, Aimilios Longo, Caterina Moscarella, Elvira Alfano, Roberto Argenziano, Giuseppe |
author_facet | Banzi, Maria De Blasio, Simona Lallas, Aimilios Longo, Caterina Moscarella, Elvira Alfano, Roberto Argenziano, Giuseppe |
author_sort | Banzi, Maria |
collection | PubMed |
description | Prior to 2011, the 1-year survival rates for patients suffering from advanced or metastatic melanoma was as low as 33%, with a median overall survival of about 9 months. Several chemotherapeutic regimens have been applied, either as monochemotherapy or as polychemotherapy, overall not resulting in an improvement of progression-free or overall survival. Novel insights into the epidemiology and biology of melanoma allowed the development of newer therapies. The discovery of mutations in BRAF, a part of the mitogen-activated protein kinase, allowed the development of two BRAF inhibitors, vemurafenib and dabrafenib, which significantly improved the outcome of metastatic melanoma treatment. This article reviews the mechanism of action, efficacy, and safety profile of dabrafenib. An in-depth knowledge of this medication will encourage clinicians to select the appropriate therapeutic strategy for each patient, as well as to prevent or adequately manage side effects, optimizing, thus, the drug’s applicability. |
format | Online Article Text |
id | pubmed-4866744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48667442016-05-25 Dabrafenib: a new opportunity for the treatment of BRAF V600-positive melanoma Banzi, Maria De Blasio, Simona Lallas, Aimilios Longo, Caterina Moscarella, Elvira Alfano, Roberto Argenziano, Giuseppe Onco Targets Ther Review Prior to 2011, the 1-year survival rates for patients suffering from advanced or metastatic melanoma was as low as 33%, with a median overall survival of about 9 months. Several chemotherapeutic regimens have been applied, either as monochemotherapy or as polychemotherapy, overall not resulting in an improvement of progression-free or overall survival. Novel insights into the epidemiology and biology of melanoma allowed the development of newer therapies. The discovery of mutations in BRAF, a part of the mitogen-activated protein kinase, allowed the development of two BRAF inhibitors, vemurafenib and dabrafenib, which significantly improved the outcome of metastatic melanoma treatment. This article reviews the mechanism of action, efficacy, and safety profile of dabrafenib. An in-depth knowledge of this medication will encourage clinicians to select the appropriate therapeutic strategy for each patient, as well as to prevent or adequately manage side effects, optimizing, thus, the drug’s applicability. Dove Medical Press 2016-05-06 /pmc/articles/PMC4866744/ /pubmed/27226731 http://dx.doi.org/10.2147/OTT.S75104 Text en © 2016 Banzi et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Banzi, Maria De Blasio, Simona Lallas, Aimilios Longo, Caterina Moscarella, Elvira Alfano, Roberto Argenziano, Giuseppe Dabrafenib: a new opportunity for the treatment of BRAF V600-positive melanoma |
title | Dabrafenib: a new opportunity for the treatment of BRAF V600-positive melanoma |
title_full | Dabrafenib: a new opportunity for the treatment of BRAF V600-positive melanoma |
title_fullStr | Dabrafenib: a new opportunity for the treatment of BRAF V600-positive melanoma |
title_full_unstemmed | Dabrafenib: a new opportunity for the treatment of BRAF V600-positive melanoma |
title_short | Dabrafenib: a new opportunity for the treatment of BRAF V600-positive melanoma |
title_sort | dabrafenib: a new opportunity for the treatment of braf v600-positive melanoma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4866744/ https://www.ncbi.nlm.nih.gov/pubmed/27226731 http://dx.doi.org/10.2147/OTT.S75104 |
work_keys_str_mv | AT banzimaria dabrafenibanewopportunityforthetreatmentofbrafv600positivemelanoma AT deblasiosimona dabrafenibanewopportunityforthetreatmentofbrafv600positivemelanoma AT lallasaimilios dabrafenibanewopportunityforthetreatmentofbrafv600positivemelanoma AT longocaterina dabrafenibanewopportunityforthetreatmentofbrafv600positivemelanoma AT moscarellaelvira dabrafenibanewopportunityforthetreatmentofbrafv600positivemelanoma AT alfanoroberto dabrafenibanewopportunityforthetreatmentofbrafv600positivemelanoma AT argenzianogiuseppe dabrafenibanewopportunityforthetreatmentofbrafv600positivemelanoma |